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FDA 510(k)

HYPO-ALLERGENIC SURGICAL GLOVES

K-Number: K900669 · 1990-04-16

Decision Date1990-04-16
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HYPO-ALLERGENIC SURGICAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Modern Rubber Industrial Co., Ltd.. It received FDA 510(k) clearance on 1990-04-16 under 510(k) number K900669. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYPO-ALLERGENIC SURGICAL GLOVES?

HYPO-ALLERGENIC SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1990-04-16. The listed applicant is Modern Rubber Industrial Co., Ltd.. The 510(k) number is K900669.

When did HYPO-ALLERGENIC SURGICAL GLOVES receive FDA 510(k) clearance?

HYPO-ALLERGENIC SURGICAL GLOVES received FDA 510(k) clearance on 1990-04-16, under 510(k) number K900669.

Who is the listed applicant for HYPO-ALLERGENIC SURGICAL GLOVES?

The FDA 510(k) record lists Modern Rubber Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYPO-ALLERGENIC SURGICAL GLOVES?

The FDA product code for HYPO-ALLERGENIC SURGICAL GLOVES is KGO.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Modern Rubber Industrial Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: KGO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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